80 FR 58600 - Listing of Color Additives Exempt From Certification; Mica-Based Pearlescent Pigments
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration Federal Register Volume 80, Issue 189 (September 30, 2015)
Food and Drug Administration
Federal Register Volume 80, Issue 189 (September 30, 2015)
| Page Range | 58600-58602 | |
| FR Document | 2015-24795 |
[Federal Register Volume 80, Number 189 (Wednesday, September 30, 2015)] [Rules and Regulations] [Pages 58600-58602] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2015-24795] [[Page 58600]] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 73 [Docket No. FDA-2015-C-1154] Listing of Color Additives Exempt From Certification; Mica-Based Pearlescent Pigments AGENCY: Food and Drug Administration, HHS. ACTION: Final rule. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (``FDA'' or ``we'') is amending the color additive regulations to provide for the safe use of mica-based pearlescent pigments prepared from titanium dioxide and mica as color additives in certain distilled spirits. This action is in response to a color additive petition (CAP) submitted by E. & J. Gallo Winery. DATES: This rule is effective November 2, 2015. See section VIII for further information on the filing of objections. Submit either electronic or written objections and requests for a hearing by October 30, 2015. ADDRESSES: You may submit either electronic or written objections and requests for a hearing, identified by Docket No. FDA-2015-C-1154, by any of the following methods: Electronic Submissions Submit electronic objections in the following way:Federal eRulemaking Portal: http://www.regulations.gov. Follow the instructions for submitting comments. Written Submissions Submit written objections in the following ways: Mail/Hand delivery/Courier (for paper or submissions): Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Instructions: All submissions received must include the Agency name and Docket No. FDA-2015-C-1154 for this rulemaking. All objections received will be posted without change to http://www.regulations.gov, including any personal information provided. For detailed instructions on submitting objections, see the ``Objections'' heading of the SUPPLEMENTARY INFORMATION section. Docket: For access to the docket to read background documents or objections received, go to http://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ``Search'' box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Salome Bhagan, Center for Food Safety and Applied Nutrition (HFS-265), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740-3835, 240-402-3041. SUPPLEMENTARY INFORMATION: I. Background In a notice published in the Federal Register on April 22, 2015 (80 FR 22449), we announced that we filed a color additive petition (CAP 5C0302) to amend the color additive regulations in Sec. 73.350 Mica- based pearlescent pigments (21 CFR 73.350). CAP 5C0302 was submitted by E. & J. Gallo Winery, c/o Keller and Heckman LLP, Three Embarcadero Center, Suite 1420, San Francisco, CA 94111 (petitioner). In CAP 5C0302, E. & J. Gallo Winery proposed to amend the color additive regulations in Sec. 73.350 to increase the maximum permitted alcohol content of distilled spirits to which mica- based pearlescent pigments may be added from 23 percent to 25 percent alcohol by volume, and to remove the current limitation for distilled spirits mixtures containing more than 5 percent wine on a proof gallon basis. The term ``distilled spirits'' is defined by the Alcohol and Tobacco Tax and Trade Bureau as ethyl alcohol, hydrated oxide of ethyl, spirits of wine, whisky, rum, brandy, gin, and other distilled spirits, including all dilutions and mixtures thereof, for nonindustrial use. The term does not include mixtures containing wine, bottled at 48 degrees of proof or less, if the mixture contains more than 50 percent wine on a proof gallon basis (27 CFR 5.11). Mica-based pearlescent pigments prepared from titanium dioxide and mica are currently approved under Sec. 73.350(c)(1)(i) for use as a color additive in amounts up to 1.25 percent, by weight, in cereals, confections and frostings, gelatin deserts, hard and soft candies (including lozenges), nutritional supplement tablets and gelatin capsules, and chewing gum. They are also approved under Sec. 73.350(c)(1)(ii) in amounts up to 0.07 percent, by weight, in: Distilled spirits containing not less than 18 percent and not more than 23 percent alcohol by volume but not including distilled spirits mixtures containing more than 5 percent wine on a proof gallon basis (Sec. 73.350(c)(1)(ii)(A)); cordials, liqueurs, flavored alcoholic malt beverages, wine coolers, and cocktails (Sec. 73.350(c)(1)(ii)(B)); and non-alcoholic cocktail mixes and mixers, such as margarita mix, Bloody Mary mix, and daiquiri mix, but excluding eggnog, tonic water, and beverages that are typically consumed without added alcohol (e.g., fruit juices, fruit juice drinks, and soft drinks) (Sec. 73.350(c)(1)(ii)(C)). The pigments also are approved under Sec. 73.350(c)(1)(iii) in egg decorating kits used for coloring the shells of eggs in amounts consistent with good manufacturing practice. Mica- based pearlescent pigments prepared from titanium dioxide on mica, iron oxide on mica, and titanium dioxide and iron oxide on mica are approved for use as a color additive in ingested drugs under Sec. 73.1350 (21 CFR 73.1350). Mica-based pearlescent pigments formed by depositing titanium or iron salts from a basic solution onto mica, followed by calcination to produce titanium dioxide or iron oxides on mica, are approved for use in contact lenses under Sec. 73.3128 (21 CFR 73.3128). The color additive that is mica-based pearlescent pigments prepared from titanium dioxide and mica will be referred hereinafter in this final rule as mica-based pearlescent pigments. II. Safety Evaluation A. Determination of Safety Under section 721(b)(4) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 379e(b)(4)), a color additive cannot be listed for a particular use unless the data and information available to FDA establishes that the color additive is safe for that use. FDA's color additive regulations in 21 CFR 70.3(i) define ``safe'' to mean that there is convincing evidence that establishes with reasonable certainty that no harm will result from the intended use of the color additive. To establish with reasonable certainty that a color additive intended for use in food is not harmful under its intended conditions of use, we consider the projected human dietary exposure to the additive, the additive's toxicological data, and other relevant information (such as published literature) available to us. We compare an individual's estimated daily intake (EDI) of the additive from all sources to an acceptable daily intake (ADI) established by toxicological data. The EDI is determined by projections based on the amount of the additive proposed for use in particular foods and on data regarding the amount consumed from all sources of the additive. We typically use the EDI for the 90th percentile consumer of a color additive as a [[Page 58601]] measure of high chronic dietary exposure. B. Safety of the Petitioned Use of the Color Additive During our safety review of the use of mica-based pearlescent pigments proposed in CAP 5C0302, we considered the exposure to the color additive from its petitioned use and from the currently permitted uses in food and ingested drugs under Sec. Sec. 73.350 and 73.1350, respectively. In estimating the cumulative estimated dietary intake (CEDI) of these pigments, we determined that the exposure to mica-based pearlescent pigments from the use in egg decorating kits used for coloring the shells of boiled eggs and in contact lenses (Sec. Sec. 73.350(c)(1)(iii) and 73.3128, respectively) is negligible and, therefore, does not contribute to the exposure. The petitioner estimated the eaters-only exposure to mica-based pearlescent pigments from the proposed use in distilled spirits containing not less than 18 percent and not more than 25 percent alcohol by volume at 0.14 grams per person per day (g/p/d) at the mean and 0.31 g/p/d at the 90th percentile for the U.S. population (Ref. 1). (An eaters-only exposure is the total of the amount of food consumed per day averaged over the number of days in the survey period by individuals consuming the food at least once during the survey period.) We conclude that the petitioner's exposure estimates are sufficiently conservative to account for the petitioned use of mica-based pearlescent pigments. Regarding cumulative exposure from the current and petitioned uses of mica-based pearlescent pigments, we note that in our recent final rule that provided for the safe use of mica-based pearlescent pigments as color additives in cordials, liqueurs, flavored alcoholic malt beverages, wine coolers, cocktails, non-alcoholic cocktail mixers and mixes, and in egg decorating kits for coloring shell eggs, we estimated the CEDI for the use of mica-based pearlescent pigments in food (Sec. 73.350) and ingested drugs (Sec. 73.1350) to be 0.25 g/p/d at the mean and 0.50 g/p/d at the 90th percentile for the U.S. population (80 FR 32303 at 32305, June 8, 2015). Since the petitioned use of mica-based pearlescent pigments will generally substitute for currently-permitted uses of mica-based pearlescent pigments in other alcoholic beverages with no change in the maximum use level of 0.07 percent by weight, we have determined that the petitioned use of mica-based pearlescent pigments will not result in an increase in consumer exposure to these pigments. Therefore, we conclude that our previous CEDI for mica-based pearlescent pigments of 0.25 g/p/d at the mean and 0.50 g/p/d at the 90th percentile for the U.S. population will remain unchanged (Ref. 1). To support the safety of the proposed use of mica-based pearlescent pigments in food, the petitioner referenced the safety determination made by FDA for previously filed petitions (70 FR 42271, July 22, 2005); (71 FR 31927, June 2, 2006); and (78 FR 35115, June 12, 2013); including our previously established ADI for mica-based pearlescent pigments of 1.8 g/p/d based on a 2-year rat carcinogenicity bioassay (71 FR 31927 at 31928). Because there is no increase in the intake of mica-based pearlescent pigments beyond a level that has already been established as safe, FDA has no concerns regarding the petitioned use of mica-based pearlescent pigments in distilled spirits containing not less than 18 percent and not more than 25 percent alcohol by volume (Ref. 2). III. Conclusion Based on the data and information in the petition and other relevant material, FDA concludes that the petitioned use of mica-based pearlescent pigments prepared from titanium dioxide and mica as a color additive at a level of up to 0.07 percent by weight in distilled spirits containing not less than 18 percent and not more than 25 percent alcohol by volume, is safe. We further conclude that the additive will achieve its intended technical effect and is suitable for the petitioned use. Therefore, we are amending the color additive regulations in part 73 as set forth in this document. In addition, based upon the factors listed in 21 CFR 71.20(b), we conclude that certification of mica-based pearlescent pigments prepared from titanium dioxide and mica is not necessary for the protection of the public health. IV. Public Disclosure In accordance with Sec. 71.15 (21 CFR 71.15), the petitions and the documents that we considered and relied upon in reaching our decision to approve the petition will be made available for public disclosure (see FOR FURTHER INFORMATION CONTACT). As provided in Sec. 71.15, we will delete from the documents any materials that are not available for public disclosure. V. Environmental Impact We previously considered the environmental effects of this rule, as stated in the April 22, 2015 notice of filing for CAP 5C0302 (80 FR 22449). We stated that we had determined, under 21 CFR 25.32(k), that this action is of a type that does not individually or cumulatively have a significant effect on the human environment such that neither an environmental assessment nor an environmental impact statement is required. We have not received any new information or comments that would affect our previous determination. VI. Paperwork Reduction Act of 1995 This final rule contains no collection of information. Therefore, clearance by the Office of Management and Budget under the Paperwork Reduction Act of 1995 is not required. VII. Section 301(ll) of the Federal Food, Drug, and Cosmetic Act Our review of this petition was limited to section 721 of the FD&C Act. This final rule is not a statement regarding compliance with other sections of the FD&C Act. For example, section 301(ll) of the FD&C Act prohibits the introduction or delivery for introduction into interstate commerce of any food that contains a drug approved under section 505 of the FD&C Act (21 U.S.C. 355), a biological product licensed under section 351 of the Public Health Service Act (42 U.S.C. 262), or a drug or biological product for which substantial clinical investigations have been instituted and their existence has been made public, unless one of the exemptions in section 301(ll)(1) to (ll)(4) of the FD&C Act applies. In our review of this petition, we did not consider whether section 301(ll) of the FD&C Act or any of its exemptions apply to food containing this additive. Accordingly, this final rule should not be construed to be a statement that a food containing this additive, if introduced or delivered for introduction into interstate commerce, would not violate section 301(ll) of the FD&C Act. Furthermore, this language is included in all color additive final rules that pertain to food and therefore should not be construed to be a statement of the likelihood that section 301(ll) of the FD&C Act applies. VIII. Objections This rule is effective as shown in the DATES section, except as to any provisions that may be stayed by the filing of proper objections. If you will be adversely affected by one or more provisions of this regulation, you may file with the Division of Dockets Management (see ADDRESSES) either electronic or written objections. You must separately number each objection, and within each numbered objection you must specify with particularity the provision(s) to which you object, and the grounds for your objection. Within [[Page 58602]] each numbered objection, you must specifically state whether you are requesting a hearing on the particular provision that you specify in that numbered objection. If you do not request a hearing for any particular objection, you waive the right to a hearing on that objection. If you request a hearing, your objection must include a detailed description and analysis of the specific factual information you intend to present in support of the objection in the event that a hearing is held. If you do not include such a description and analysis for any particular objection, you waive the right to a hearing on the objection. It is only necessary to send one set of documents. Identify documents with the docket number found in brackets in the heading of this document. Any objections received in response to the regulation may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday, and will be posted to the docket at http://www.regulations.gov. We will publish notice of the objections that we have received or lack thereof in the Federal Register. IX. References The following references have been placed on display in the Division of Dockets Management (see ADDRESSES) and may be seen by interested persons between 9 a.m. and 4 p.m., Monday through Friday and are available electronically at http://www.regulations.gov. 1. FDA Memorandum from H. Lee, Chemistry Review Group, Division of Petition Review, to S. Bhagan, Regulatory Group I, Division of Petition Review, May 19, 2015. 2. FDA Memorandum from S. Park, Toxicology Team, Division of Petition Review, to S. Bhagan, Regulatory Group I, Division of Petition Review, June 8, 2015. List of Subjects in 21 CFR Part 73 Color additives, Cosmetics, Drugs, Medical devices. Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs, and redelegated to the Director, Center for Food Safety and Applied Nutrition, 21 CFR part 73 is amended as follows: PART 73--LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION 0 1. The authority citation for 21 CFR part 73 continues to read as follows: Authority: 21 U.S.C. 321, 341, 342, 343, 348, 351, 352, 355, 361, 362, 371, 379e. 0 2. Section 73.350 is amended by revising paragraph (c)(1)(ii)(A) to read as follows: Sec. 73.350 Mica-based pearlescent pigments. * * * * * (c) * * * (1) * * * (ii) * * * (A) Distilled spirits containing not less than 18 percent and not more than 25 percent alcohol by volume. * * * * * Dated: September 25, 2015. Susan Bernard, Director, Office of Regulations, Policy and Social Sciences, Center for Food Safety and Applied Nutrition. [FR Doc. 2015-24795 Filed 9-29-15; 8:45 am] BILLING CODE 4164-01-P
![58600 Federal Register / Vol. 80, No. 189 / Wednesday, September 30, 2015 / Rules and Regulations
DEPARTMENT OF HEALTH AND heading of this document, into the coolers, and cocktails
HUMAN SERVICES ‘‘Search’’ box and follow the prompts (§ 73.350(c)(1)(ii)(B)); and non-alcoholic
and/or go to the Division of Dockets cocktail mixes and mixers, such as
Food and Drug Administration Management, 5630 Fishers Lane, Rm. margarita mix, Bloody Mary mix, and
1061, Rockville, MD 20852. daiquiri mix, but excluding eggnog,
21 CFR Part 73 FOR FURTHER INFORMATION CONTACT: tonic water, and beverages that are
[Docket No. FDA–2015–C–1154] Salome Bhagan, Center for Food Safety typically consumed without added
and Applied Nutrition (HFS–265), Food alcohol (e.g., fruit juices, fruit juice
Listing of Color Additives Exempt and Drug Administration, 5100 Paint drinks, and soft drinks)
From Certification; Mica-Based Branch Pkwy., College Park, MD 20740– (§ 73.350(c)(1)(ii)(C)). The pigments also
Pearlescent Pigments 3835, 240–402–3041. are approved under § 73.350(c)(1)(iii) in
SUPPLEMENTARY INFORMATION:
egg decorating kits used for coloring the
AGENCY: Food and Drug Administration, shells of eggs in amounts consistent
HHS. I. Background with good manufacturing practice.
ACTION: Final rule. In a notice published in the Federal Mica-based pearlescent pigments
Register on April 22, 2015 (80 FR prepared from titanium dioxide on
SUMMARY: The Food and Drug mica, iron oxide on mica, and titanium
Administration (‘‘FDA’’ or ‘‘we’’) is 22449), we announced that we filed a
color additive petition (CAP 5C0302) to dioxide and iron oxide on mica are
amending the color additive regulations approved for use as a color additive in
to provide for the safe use of mica-based amend the color additive regulations in
§ 73.350 Mica-based pearlescent ingested drugs under § 73.1350 (21 CFR
pearlescent pigments prepared from 73.1350). Mica-based pearlescent
titanium dioxide and mica as color pigments (21 CFR 73.350).
CAP 5C0302 was submitted by E. & J. pigments formed by depositing titanium
additives in certain distilled spirits. or iron salts from a basic solution onto
This action is in response to a color Gallo Winery, c/o Keller and Heckman
LLP, Three Embarcadero Center, Suite mica, followed by calcination to
additive petition (CAP) submitted by E. produce titanium dioxide or iron oxides
& J. Gallo Winery. 1420, San Francisco, CA 94111
(petitioner). In CAP 5C0302, E. & J. on mica, are approved for use in contact
DATES: This rule is effective November lenses under § 73.3128 (21 CFR
2, 2015. See section VIII for further Gallo Winery proposed to amend the
color additive regulations in § 73.350 to 73.3128). The color additive that is
information on the filing of objections. mica-based pearlescent pigments
Submit either electronic or written increase the maximum permitted
alcohol content of distilled spirits to prepared from titanium dioxide and
objections and requests for a hearing by mica will be referred hereinafter in this
October 30, 2015. which mica-based pearlescent pigments
may be added from 23 percent to 25 final rule as mica-based pearlescent
ADDRESSES: You may submit either pigments.
percent alcohol by volume, and to
electronic or written objections and
remove the current limitation for II. Safety Evaluation
requests for a hearing, identified by
distilled spirits mixtures containing
Docket No. FDA–2015–C–1154, by any A. Determination of Safety
more than 5 percent wine on a proof
of the following methods: Under section 721(b)(4) of the Federal
gallon basis. The term ‘‘distilled spirits’’
Electronic Submissions is defined by the Alcohol and Tobacco Food, Drug, and Cosmetic Act (the
Submit electronic objections in the Tax and Trade Bureau as ethyl alcohol, FD&C Act) (21 U.S.C. 379e(b)(4)), a color
following way: hydrated oxide of ethyl, spirits of wine, additive cannot be listed for a particular
• Federal eRulemaking Portal: http:// whisky, rum, brandy, gin, and other use unless the data and information
www.regulations.gov. Follow the distilled spirits, including all dilutions available to FDA establishes that the
instructions for submitting comments. and mixtures thereof, for nonindustrial color additive is safe for that use. FDA’s
use. The term does not include mixtures color additive regulations in 21 CFR
Written Submissions containing wine, bottled at 48 degrees of 70.3(i) define ‘‘safe’’ to mean that there
Submit written objections in the proof or less, if the mixture contains is convincing evidence that establishes
following ways: more than 50 percent wine on a proof with reasonable certainty that no harm
• Mail/Hand delivery/Courier (for gallon basis (27 CFR 5.11). will result from the intended use of the
paper or submissions): Division of Mica-based pearlescent pigments color additive. To establish with
Dockets Management (HFA–305), Food prepared from titanium dioxide and reasonable certainty that a color
and Drug Administration, 5630 Fishers mica are currently approved under additive intended for use in food is not
Lane, Rm. 1061, Rockville, MD 20852. § 73.350(c)(1)(i) for use as a color harmful under its intended conditions
Instructions: All submissions received additive in amounts up to 1.25 percent, of use, we consider the projected human
must include the Agency name and by weight, in cereals, confections and dietary exposure to the additive, the
Docket No. FDA–2015–C–1154 for this frostings, gelatin deserts, hard and soft additive’s toxicological data, and other
rulemaking. All objections received will candies (including lozenges), nutritional relevant information (such as published
be posted without change to http:// supplement tablets and gelatin capsules, literature) available to us. We compare
www.regulations.gov, including any and chewing gum. They are also an individual’s estimated daily intake
personal information provided. For approved under § 73.350(c)(1)(ii) in (EDI) of the additive from all sources to
detailed instructions on submitting amounts up to 0.07 percent, by weight, an acceptable daily intake (ADI)
objections, see the ‘‘Objections’’ heading in: Distilled spirits containing not less established by toxicological data. The
mstockstill on DSK4VPTVN1PROD with RULES
of the SUPPLEMENTARY INFORMATION than 18 percent and not more than 23 EDI is determined by projections based
section. percent alcohol by volume but not on the amount of the additive proposed
Docket: For access to the docket to including distilled spirits mixtures for use in particular foods and on data
read background documents or containing more than 5 percent wine on regarding the amount consumed from
objections received, go to http:// a proof gallon basis all sources of the additive. We typically
www.regulations.gov and insert the (§ 73.350(c)(1)(ii)(A)); cordials, liqueurs, use the EDI for the 90th percentile
docket number, found in brackets in the flavored alcoholic malt beverages, wine consumer of a color additive as a
VerDate Sep<11>2014 17:12 Sep 29, 2015 Jkt 235001 PO 00000 Frm 00028 Fmt 4700 Sfmt 4700 E:\FR\FM\30SER1.SGM 30SER1](https://thefederalregister.org/doc/80_FR_58789/page/1.svg)
![58602 Federal Register / Vol. 80, No. 189 / Wednesday, September 30, 2015 / Rules and Regulations
each numbered objection, you must ■ 2. Section 73.350 is amended by • Federal eRulemaking Portal: http://
specifically state whether you are revising paragraph (c)(1)(ii)(A) to read as www.regulations.gov. Follow the
requesting a hearing on the particular follows: instructions for submitting comments.
provision that you specify in that Comments submitted electronically,
numbered objection. If you do not § 73.350 Mica-based pearlescent including attachments, to http://
pigments.
request a hearing for any particular www.regulations.gov will be posted to
objection, you waive the right to a * * * * * the docket unchanged. Because your
hearing on that objection. If you request (c) * * * comment will be made public, you are
a hearing, your objection must include (1) * * * solely responsible for ensuring that your
a detailed description and analysis of (ii) * * * comment does not include any
the specific factual information you (A) Distilled spirits containing not confidential information that you or a
intend to present in support of the less than 18 percent and not more than third party may not wish to be posted,
objection in the event that a hearing is 25 percent alcohol by volume. such as medical information, your or
held. If you do not include such a * * * * * anyone else’s Social Security number, or
description and analysis for any Dated: September 25, 2015. confidential business information, such
particular objection, you waive the right Susan Bernard,
as a manufacturing process. Please note
to a hearing on the objection. that if you include your name, contact
It is only necessary to send one set of Director, Office of Regulations, Policy and
information, or other information that
Social Sciences, Center for Food Safety and
documents. Identify documents with the identifies you in the body of your
Applied Nutrition.
docket number found in brackets in the comments, that information will be
[FR Doc. 2015–24795 Filed 9–29–15; 8:45 am]
heading of this document. Any posted on http://www.regulations.gov.
objections received in response to the BILLING CODE 4164–01–P
• If you want to submit a comment
regulation may be seen in the Division with confidential information that you
of Dockets Management between 9 a.m. do not wish to be made available to the
DEPARTMENT OF HEALTH AND
and 4 p.m., Monday through Friday, and public, submit the comment as a
will be posted to the docket at http:// HUMAN SERVICES
written/paper submission and in the
www.regulations.gov. We will publish Food and Drug Administration manner detailed (see ‘‘Written/Paper
notice of the objections that we have Submissions’’ and ‘‘Instructions’’).
received or lack thereof in the Federal 21 CFR Part 558
Register. Written/Paper Submissions
[Docket No. FDA–2010–N–0155] Submit written/paper submissions as
IX. References follows:
The following references have been Veterinary Feed Directive Regulation • Mail/Hand delivery/Courier (for
placed on display in the Division of Questions and Answers; Small Entity written/paper submissions): Division of
Dockets Management (see ADDRESSES) Compliance Guide; Guidance for Dockets Management (HFA–305), Food
and may be seen by interested persons Industry; Availability and Drug Administration, 5630 Fishers
between 9 a.m. and 4 p.m., Monday Lane, Rm. 1061, Rockville, MD 20852.
through Friday and are available AGENCY: Food and Drug Administration, • For written/paper comments
electronically at http:// HHS. submitted to the Division of Dockets
www.regulations.gov. ACTION: Notification of availability. Management, FDA will post your
1. FDA Memorandum from H. Lee, Chemistry comment, as well as any attachments,
SUMMARY: The Food and Drug
Review Group, Division of Petition except for information submitted,
Administration (FDA) is announcing the
Review, to S. Bhagan, Regulatory Group marked and identified, as confidential,
availability of a small entity compliance
I, Division of Petition Review, May 19, if submitted as detailed in
2015. guide and guidance for industry #120
‘‘Instructions.’’
2. FDA Memorandum from S. Park, entitled ‘‘Veterinary Feed Directive Instructions: All submissions received
Toxicology Team, Division of Petition Regulation Questions and Answers.’’ must include the Docket No. FDA–
Review, to S. Bhagan, Regulatory Group This guidance aids industry in 2010–N–0155 for ‘‘Veterinary Feed
I, Division of Petition Review, June 8, complying with the requirements of the
2015. Directive Regulation Questions and
Veterinary Feed Directive (VFD) final Answers; Small Entity Compliance
List of Subjects in 21 CFR Part 73 rule that published in the Federal Guide; Guidance for Industry;
Register on June 3, 2015. The purpose Availability.’’ Received comments will
Color additives, Cosmetics, Drugs,
of this document is to describe the be placed in the docket and, except for
Medical devices.
Veterinary Feed Directive requirements those submitted as ‘‘Confidential
Therefore, under the Federal Food, for veterinarians, feed manufacturers
Drug, and Cosmetic Act and under Submissions,’’ publicly viewable at
and other distributors, animal http://www.regulations.gov or at the
authority delegated to the Commissioner producers, and other parties involved in
of Food and Drugs, and redelegated to Division of Dockets Management
the distribution or use of medicated feed between 9 a.m. and 4 p.m., Monday
the Director, Center for Food Safety and containing a Veterinary Feed Directive
Applied Nutrition, 21 CFR part 73 is through Friday.
drug (VFD feed). • Confidential Submissions—To
amended as follows:
DATES: Submit either electronic or submit a comment with confidential
PART 73—LISTING OF COLOR written comments on Agency guidances information that you do not wish to be
mstockstill on DSK4VPTVN1PROD with RULES
ADDITIVES EXEMPT FROM at any time. made publicly available, submit your
CERTIFICATION ADDRESSES: You may submit comments comments only as a written/paper
as follows: submission. You should submit two
■ 1. The authority citation for 21 CFR copies total. One copy will include the
part 73 continues to read as follows: Electronic Submissions information you claim to be confidential
Authority: 21 U.S.C. 321, 341, 342, 343, Submit electronic comments in the with a heading or cover note that states
348, 351, 352, 355, 361, 362, 371, 379e. following way: ‘‘THIS DOCUMENT CONTAINS
VerDate Sep<11>2014 17:12 Sep 29, 2015 Jkt 235001 PO 00000 Frm 00030 Fmt 4700 Sfmt 4700 E:\FR\FM\30SER1.SGM 30SER1](https://thefederalregister.org/doc/80_FR_58789/page/3.svg)
Document Created: 2015-12-15 09:32:26
Document Modified: 2015-12-15 09:32:26
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Rules and Regulations | |
| Action | Final rule. | |
| Dates | This rule is effective November 2, 2015. See section VIII for further information on the filing of objections. Submit either electronic or written objections and requests for a hearing by October 30, 2015. | |
| Contact | Salome Bhagan, Center for Food Safety and Applied Nutrition (HFS-265), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740-3835, 240-402-3041. | |
| FR Citation | 80 FR 58600 | |
| CFR Associated | Color Additives; Cosmetics; Drugs and Medical Devices |
2025 Federal Register | Disclaimer | Privacy Policy
USC | CFR | eCFR